KEGG   PATHWAY: msto00984
Entry
msto00984                   Pathway                                
Name
Steroid degradation - Mycobacterium stomatepiae
Class
Metabolism; Xenobiotics biodegradation and metabolism
Pathway map
msto00984  Steroid degradation
msto00984

Other DBs
GO: 0006707
Organism
Mycobacterium stomatepiae [GN:msto]
Gene
MSTO_00210  [KO:K00632] [EC:2.3.1.16]
MSTO_06210  echA13_1; putative enoyl-CoA hydratase EchA13 [KO:K28232]
MSTO_06820  [KO:K15981] [EC:1.14.15.29]
MSTO_08390  [KO:K05898] [EC:1.3.99.4]
MSTO_08490  [KO:K18688] [EC:6.2.1.42]
MSTO_09020  [KO:K22818] [EC:1.3.99.-]
MSTO_09170  [KO:K16047] [EC:1.14.14.12]
MSTO_09180  [KO:K16049] [EC:1.13.11.25]
MSTO_09240  [KO:K15982] [EC:1.14.15.30]
MSTO_09250  [KO:K05898] [EC:1.3.99.4]
MSTO_14790  [KO:K18688] [EC:6.2.1.42]
MSTO_16460  [KO:K15982] [EC:1.14.15.30]
MSTO_16640  ltp1_1; lipid-transfer protein [KO:K00632] [EC:2.3.1.16]
MSTO_20030  [KO:K16047] [EC:1.14.14.12]
MSTO_23740  echA13_2; putative enoyl-CoA hydratase EchA13 [KO:K28232]
MSTO_25320  [KO:K00632] [EC:2.3.1.16]
MSTO_25520  [KO:K16051] [EC:1.3.99.5]
MSTO_26070  [KO:K05898] [EC:1.3.99.4]
MSTO_27440  choD; cholesterol oxidase [KO:K03333] [EC:1.1.3.6]
MSTO_27530  ltp1_2; lipid-transfer protein [KO:K00632] [EC:2.3.1.16]
MSTO_36070  [KO:K15981] [EC:1.14.15.29]
MSTO_36740  [KO:K28224]
MSTO_41650  [KO:K15982] [EC:1.14.15.30]
MSTO_44560  fadE34; acyl-CoA dehydrogenase [KO:K22820] [EC:1.3.99.-]
MSTO_44590  hmp; 3-ketosteroid-9-alpha-hydroxylase reductase subunit [KO:K15983] [EC:1.14.15.30]
MSTO_44600  [KO:K16047] [EC:1.14.14.12]
MSTO_44610  hsaD; 4,5:9,10-diseco-3-hydroxy-5,9, 17-trioxoandrosta-1 (10),2-diene-4-oate hydrolase [KO:K16050] [EC:3.7.1.17]
MSTO_44620  hsaC; iron-dependent extradiol dioxygenase [KO:K16049] [EC:1.13.11.25]
MSTO_44630  [KO:K16048] [EC:1.5.1.-]
MSTO_44720  fadE33; acyl-CoA dehydrogenase [KO:K28221]
MSTO_44730  fadE32; acyl-CoA dehydrogenase [KO:K28231]
MSTO_44740  fadE31; acyl-CoA dehydrogenase [KO:K28230]
MSTO_44750  fadD3; 3-[(3aS,4S,7aS)-7a-methyl-1,5-dioxo-octahydro-1H-inden-4-yl]propanoyl:CoA ligase [KO:K18687] [EC:6.2.1.41]
MSTO_44760  fadE30; acyl-CoA dehydrogenase [KO:K28222]
MSTO_44770  [KO:K28220]
MSTO_44790  fadA6; acetyl-CoA acetyltransferase [KO:K00632] [EC:2.3.1.16]
MSTO_44800  [KO:K28226]
MSTO_44810  [KO:K28229]
MSTO_44820  [KO:K28228]
MSTO_44830  [KO:K28227]
MSTO_44850  [KO:K28225]
MSTO_44880  [KO:K00632] [EC:2.3.1.16]
MSTO_44890  [KO:K15981] [EC:1.14.15.29]
MSTO_44900  fadE28; acyl-CoA dehydrogenase FadE28 [KO:K22821] [EC:1.3.99.-]
MSTO_44910  fadE29; acyl-CoA dehydrogenase FadE29 [KO:K22822] [EC:1.3.99.-]
MSTO_44920  [KO:K25621]
MSTO_44930  [KO:K25622]
MSTO_44940  ltp2; lipid-transfer protein [KO:K25623]
MSTO_44960  [KO:K28218]
MSTO_44970  kstD; 3-oxosteroid 1-dehydrogenase [KO:K05898] [EC:1.3.99.4]
MSTO_45060  kshA; 3-ketosteroid-9-alpha-monooxygenase, oxygenase component [KO:K15982] [EC:1.14.15.30]
MSTO_45110  [KO:K01822] [EC:5.3.3.1]
MSTO_45170  cyp142; putative cytochrome P450 142 [KO:K16046] [EC:1.14.15.28]
MSTO_45210  fadD19; long-chain-fatty-acid--CoA/3-oxocholest-4-en-26-o ate--CoA ligase [KO:K18688] [EC:6.2.1.42]
MSTO_45310  fadE27; acyl-CoA dehydrogenase [KO:K22819] [EC:1.3.99.-]
MSTO_45320  fadE26; acyl-CoA dehydrogenase FadE26 [KO:K22818] [EC:1.3.99.-]
MSTO_45340  [KO:K28219]
MSTO_45770  [KO:K01822] [EC:5.3.3.1]
MSTO_47140  [KO:K05898] [EC:1.3.99.4]
MSTO_47510  [KO:K00632] [EC:2.3.1.16]
MSTO_48100  [KO:K18687] [EC:6.2.1.41]
MSTO_48150  far; fatty-acid-CoA racemase [KO:K01796] [EC:5.1.99.4]
MSTO_51430  [KO:K16045] [EC:1.1.1.145 5.3.3.1]
MSTO_52010  [KO:K00632] [EC:2.3.1.16]
MSTO_52490  [KO:K22819] [EC:1.3.99.-]
MSTO_52520  [KO:K22818] [EC:1.3.99.-]
MSTO_53860  [KO:K01822] [EC:5.3.3.1]
MSTO_54980  [KO:K18688] [EC:6.2.1.42]
MSTO_55690  [KO:K16050] [EC:3.7.1.17]
MSTO_59390  [KO:K01796] [EC:5.1.99.4]
MSTO_59890  [KO:K01796] [EC:5.1.99.4]
Compound
C00022  Pyruvate
C00024  Acetyl-CoA
C00091  Succinyl-CoA
C00100  Propanoyl-CoA
C00187  Cholesterol
C00280  Androstenedione
C00479  Propanal
C00535  Testosterone
C00599  Cholest-4-en-3-one
C00674  5alpha-Androstane-3,17-dione
C01227  Dehydroepiandrosterone
C04793  3,4-Dihydroxy-9,10-secoandrosta-1,3,5(10)-triene-9,17-dione
C04844  3-Hydroxy-5,9,17-trioxo-4,5:9,10-disecoandrosta-1(10),2-dien-4-oate
C06762  4-Hydroxy-2-oxohexanoic acid
C07635  Epiandrosterone
C11354  2-Hydroxy-cis-hex-2,4-dienoate
C14909  9alpha-Hydroxyandrosta-1,4-diene-3,17-dione
C19944  3-Hydroxy-9,10-secoandrosta-1,3,5(10)-triene-9,17-dione
C20144  Androsta-1,4-diene-3,17-dione
C20199  3-[(3aS,4S,7aS)-7a-Methyl-1,5-dioxo-octahydro-1H-inden-4-yl]propanoate
C20252  5-Androstene-3,17-dione
C20838  3-[(3aS,4S,7aS)-7a-Methyl-1,5-dioxo-octahydro-1H-inden-4-yl]propanoyl-CoA
C20839  (25R)-3-Oxocholest-4-en-26-oate
C20840  (25S)-3-Oxocholest-4-en-26-oyl-CoA
C21076  Delta4-Dafachronic acid
C21906  3-Oxochol-4-en-24-oyl-CoA
C23003  3-[(3aS,4S,5R,7aS)-5-Hydroxy-7a-methyl-1-oxooctahydro-1H-inden-4-yl]propanoyl-CoA
C23004  (2E)-3-[(3aS,4S,5R,7aS)-5-Hydroxy-7a-methyl-1-oxooctahydro-1H-inden-4-yl]prop-2-enoyl-CoA
C23005  3-[(3aS,4S,5R,7aS)-5-Hydroxy-7a-methyl-1-oxooctahydro-1H-inden-4-yl]-3-hydroxypropanoyl-CoA
C23006  3-[(3aS,4S,5R,7aS)-5-Hydroxy-7a-methyl-1-oxooctahydro-1H-inden-4-yl]-3-oxopropanoyl-CoA
C23007  (3aS,4S,5R,7aS)-5-Hydroxy-7a-methyl-1-oxooctahydro-1H-indene-4-carboxyl-CoA
C23009  (7aS)-7a-Methyl-1,5-dioxo-2,3,5,6,7,7a-hexahydro-1H-indene-4-carboxyl-CoA
C23010  3-Oxocholest-4,24-dien-26-oyl-CoA
C23011  (25R)-3-Oxocholest-4-en-26-oyl-CoA
C23012  24-Hydroxy-3-oxocholest-4-en-26-oyl-CoA
C23013  3,24-Dioxocholest-4-en-26-oyl-CoA
C23014  3-Oxochol-4,22-dien-24-oyl-CoA
C23015  (22S)-Hydroxy-3-oxochol-4-en-24-oyl-CoA
C23016  3,22-Dioxochol-4-en-24-oyl-CoA
C23017  3-Oxopregnene-20-carboxyl-CoA
C23018  3-Oxo-4,17-pregnadiene-20-carboxyl-CoA
C23019  17-Hydroxy-3-oxo-4-pregnene-20-carboxyl-CoA
C23020  (3R)-2-(2-carboxyethyl)-3-methyl-6-oxocyclohex-1-ene-1-carboxyl-CoA
C23021  9-Carboxy-6-methyl-3,7-dioxononanoyl-CoA
C23022  7-Carboxy-4-methyl-5-oxoheptanoyl-CoA
C23023  (2E)-7-Carboxy-4-methyl-5-oxohept-2-enoyl-CoA
C23024  7-Carboxy-3-hydroxy-4-methyl-5-oxoheptanoyl-CoA
C23025  7-Carboxy-4-methyl-3,5-dioxoheptanoyl-CoA
C23026  5-Carboxy-2-methyl-3-oxopentanoyl-CoA
Reference
  Authors
Olivera ER, Luengo JM.
  Title
Steroids as Environmental Compounds Recalcitrant to Degradation: Genetic  Mechanisms of Bacterial Biodegradation Pathways.
  Journal
Genes (Basel) 10 (2019)
DOI:10.3390/genes10070512
Reference
  Authors
Horinouchi M, Hayashi T, Kudo T
  Title
Steroid degradation in Comamonas testosteroni.
  Journal
J Steroid Biochem Mol Biol 129:4-14 (2012)
DOI:10.1016/j.jsbmb.2010.10.008
Reference
  Authors
Horinouchi M, Kurita T, Hayashi T, Kudo T
  Title
Steroid degradation genes in Comamonas testosteroni TA441: Isolation of genes encoding a Delta4(5)-isomerase and 3alpha- and 3beta-dehydrogenases and evidence for a 100 kb steroid degradation gene hot spot.
  Journal
J Steroid Biochem Mol Biol 122:253-63 (2010)
DOI:10.1016/j.jsbmb.2010.06.002
Reference
  Authors
Horinouchi M, Hayashi T.
  Title
Identification of the Coenzyme A (CoA) Ester Intermediates and Genes Involved in  the Cleavage and Degradation of the Steroidal C-Ring by Comamonas testosteroni  TA441.
  Journal
Appl Environ Microbiol 87:e0110221 (2021)
DOI:10.1128/AEM.01102-21
Reference
  Authors
Horinouchi M, Hayashi T.
  Title
Comprehensive summary of steroid metabolism in Comamonas testosteroni TA441:  entire degradation process of basic four rings and removal of C12 hydroxyl group.
  Journal
Appl Environ Microbiol 89:e0014323 (2023)
DOI:10.1128/aem.00143-23
Reference
  Authors
Ouellet H, Johnston JB, de Montellano PR
  Title
Cholesterol catabolism as a therapeutic target in Mycobacterium tuberculosis.
  Journal
Trends Microbiol 19:530-9 (2011)
DOI:10.1016/j.tim.2011.07.009
Reference
  Authors
Van der Geize R, Yam K, Heuser T, Wilbrink MH, Hara H, Anderton MC, Sim E, Dijkhuizen L, Davies JE, Mohn WW, Eltis LD
  Title
A gene cluster encoding cholesterol catabolism in a soil actinomycete provides insight into Mycobacterium tuberculosis survival in macrophages.
  Journal
Proc Natl Acad Sci U S A 104:1947-52 (2007)
DOI:10.1073/pnas.0605728104
Reference
  Authors
Thomas ST, VanderVen BC, Sherman DR, Russell DG, Sampson NS
  Title
Pathway profiling in Mycobacterium tuberculosis: elucidation of cholesterol-derived catabolite and enzymes that catalyze its metabolism.
  Journal
J Biol Chem 286:43668-78 (2011)
DOI:10.1074/jbc.M111.313643
Reference
  Authors
Crowe AM, Casabon I, Brown KL, Liu J, Lian J, Rogalski JC, Hurst TE, Snieckus V, Foster LJ, Eltis LD.
  Title
Catabolism of the Last Two Steroid Rings in Mycobacterium tuberculosis and Other  Bacteria.
  Journal
mBio 8 (2017)
DOI:10.1128/mBio.00321-17
Reference
  Authors
Yuan T, Werman JM, Yin X, Yang M, Garcia-Diaz M, Sampson NS.
  Title
Enzymatic beta-Oxidation of the Cholesterol Side Chain in Mycobacterium tuberculosis  Bifurcates Stereospecifically at Hydration of 3-Oxo-cholest-4,22-dien-24-oyl-CoA.
  Journal
ACS Infect Dis 7:1739-1751 (2021)
DOI:10.1021/acsinfecdis.1c00069
Related
pathway
msto00010  Glycolysis / Gluconeogenesis
msto00020  Citrate cycle (TCA cycle)
msto00100  Steroid biosynthesis
msto00640  Propanoate metabolism
KO pathway
ko00984   

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